9701 · 35.1
Condensation polymerisation
Monomers with two functional groups join end-to-end to form a long polymer chain. Each time a link is made, a small molecule like water is eliminated.
Need to know
What you need to know
- Polyamides contain the repeating amide linkage: $-CONH-$.
- They are formed from monomers containing amine ($-NH_2$) and carboxylic acid ($-COOH$) groups.
- The polymer chains are held together by strong intermolecular hydrogen bonds between the polar $C=O$ and $N-H$ groups.
- This extensive hydrogen bonding gives polyamides high melting points and high tensile strength, making them suitable for fibres and ropes.
Explanation
Building Chains, Losing Molecules
- A small molecule, such as water (H₂O) or hydrogen chloride (HCl), is eliminated every time two monomers join.
- Polyesters form when a dicarboxylic acid and a diol monomer react, creating a repeating ester linkage (–COO–).
- Polyamides form from a diamine and a dicarboxylic acid (like Nylon), or from self-reacting amino acids (like proteins), creating a repeating amide linkage (–CONH–).
- To draw the polymer, identify the repeating unit formed after the small molecule is removed, and place it in square brackets with continuation bonds.